Search details
1.
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.
Blood
; 137(26): 3660-3669, 2021 07 01.
Article
in English
| MEDLINE | ID: mdl-33763700
2.
Lack of the multidrug transporter MRP4/ABCC4 defines the PEL-negative blood group and impairs platelet aggregation.
Blood
; 135(6): 441-448, 2020 02 06.
Article
in English
| MEDLINE | ID: mdl-31826245
3.
Renal allograft DARCness in subclinical acute and chronic active ABMR.
Transpl Int
; 34(8): 1494-1505, 2021 Aug.
Article
in English
| MEDLINE | ID: mdl-33983671
4.
A new efficient tool for non-invasive diagnosis of fetomaternal platelet antigen incompatibility.
Br J Haematol
; 190(5): 787-798, 2020 09.
Article
in English
| MEDLINE | ID: mdl-32266719
5.
Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.
Blood
; 125(23): 3651-4, 2015 Jun 04.
Article
in English
| MEDLINE | ID: mdl-25896650
6.
Lethal autoimmune hemagglutination due to an immunoglobulin A autoagglutinin with Band 3 specificity.
Transfusion
; 54(8): 1988-95, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24697848
7.
Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.
Hum Mutat
; 34(1): 221-8, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23125034
8.
Activity and distribution of intracellular carbonic anhydrase II and their effects on the transport activity of anion exchanger AE1/SLC4A1.
J Physiol
; 591(20): 4963-82, 2013 Oct 15.
Article
in English
| MEDLINE | ID: mdl-23878365
9.
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
Am J Hum Genet
; 87(5): 721-7, 2010 Nov 12.
Article
in English
| MEDLINE | ID: mdl-21055716
10.
In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.
Am J Hematol
; 88(5): 343-9, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23417980
11.
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
EMBO Mol Med
; 15(3): e16320, 2023 03 08.
Article
in English
| MEDLINE | ID: mdl-36695047
12.
Blood group genotyping by high-throughput DNA analysis applied to 356 reagent red blood cell samples.
Transfusion
; 51(1): 36-42, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-20707859
13.
Generation and characterisation of Rhd and Rhag null mice.
Br J Haematol
; 148(1): 161-72, 2010 Jan.
Article
in English
| MEDLINE | ID: mdl-19807729
14.
Intercellular adhesion molecule-4 and CD36 are implicated in the abnormal adhesiveness of sickle cell SAD mouse erythrocytes to endothelium.
Haematologica
; 95(5): 730-7, 2010 May.
Article
in English
| MEDLINE | ID: mdl-20015873
15.
Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a-) phenotype in a West African woman.
Transfusion
; 55(11): 2766-7, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-26173500
16.
A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.
Transfusion
; 50(10): 2106-16, 2010 Oct.
Article
in English
| MEDLINE | ID: mdl-20492605
17.
Functional analysis of human RhCG: comparison with E. coli ammonium transporter reveals similarities in the pore and differences in the vestibule.
Am J Physiol Cell Physiol
; 297(3): C537-47, 2009 Sep.
Article
in English
| MEDLINE | ID: mdl-19553567
18.
RhAG protein of the Rhesus complex is a CO2 channel in the human red cell membrane.
FASEB J
; 22(1): 64-73, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-17712059
19.
Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome.
Transfusion
; 49(3): 479-84, 2009 Mar.
Article
in English
| MEDLINE | ID: mdl-19040496
20.
Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.
Transfusion
; 49(3): 495-504, 2009 Mar.
Article
in English
| MEDLINE | ID: mdl-19040491